| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4395 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | A/C | isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD |
| S4396 | missense_variant | MTHFR | NM_005957.5:c.1298A>C | A/C | isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD |